Tardieu D, Thouvenot N, Fargier C, de Saqui-Sannes P, Petit C
Department des Sciences Biologiques et Fonctionnelles, Ecole Nationale Veterinaire, Toulouse, France.
Vet Hum Toxicol. 1996 Dec;38(6):454-6.
The mechanism of metaldehyde toxicity is unclear. It may be due to the compound itself or, at least in part, to acetaldehyde resulting from the hydrolysis of metaldehyde in the stomach. In this study, we orally dosed rats with twice the LD50 of metaldehyde following no pretreatment (control) or pretreatment with 1 of 3 different cytochrome P-450 inducers either phenobarbital or o,p'-DDD (inducers of cytochromes P-450 IIB and IIIA) or 3-methylcholanthrene (an inducer of P-450 IA). Our results show strong protection against metaldehyde poisoning afforded by the phenobarbital-DDD P-450 inducers, but only weak protection with 3-methylcholanthrene pretreatment. Acetaldehyde administered at the same molarity failed to produce the clinical signs of metaldehyde toxicity and no clinical differences were observed between any of the pretreated groups.
聚乙醛毒性的机制尚不清楚。这可能是由于该化合物本身,或者至少部分是由于聚乙醛在胃中水解产生的乙醛。在本研究中,我们在未进行预处理(对照)或用三种不同的细胞色素P - 450诱导剂之一(苯巴比妥或邻,对'-滴滴滴(细胞色素P - 450 IIB和IIIA的诱导剂)或3 - 甲基胆蒽(P - 450 IA的诱导剂))进行预处理后,给大鼠口服两倍LD50的聚乙醛。我们的结果表明,苯巴比妥 - 滴滴滴P - 450诱导剂对聚乙醛中毒有很强的保护作用,但3 - 甲基胆蒽预处理只有微弱的保护作用。以相同摩尔浓度给予的乙醛未能产生聚乙醛毒性的临床症状,并且在任何预处理组之间未观察到临床差异。